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383090

Sigma-Aldrich

Ammonium cerium(IV) sulfate dihydrate

ACS reagent, ≥94%

Synonym(s):

Ceric ammonium sulfate, Cerium(IV) ammonium sulfate

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$163.00
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$531.00

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Estimated to ship onMay 03, 2025


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100 G
$163.00
500 G
$531.00

About This Item

Linear Formula:
Ce(NH4)4(SO4)4 · 2H2O
CAS Number:
Molecular Weight:
632.55
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NB.24
assay:
≥94%
grade:
ACS reagent
form:
powder or crystals

$163.00


Estimated to ship onMay 03, 2025


Request a Bulk Order

grade

ACS reagent

Quality Level

assay

≥94%

form

powder or crystals

reaction suitability

reagent type: catalyst
core: cerium

impurities

≤0.05% insol. dil. H2SO4

mp

130 °C (lit.)

anion traces

phosphate (PO43-): ≤0.03%

cation traces

Fe: ≤0.01%

SMILES string

N.N.N.N.O.O.[Ce+4].OS([O-])(=O)=O.OS([O-])(=O)=O.OS([O-])(=O)=O.OS([O-])(=O)=O

InChI

1S/Ce.4H3N.4H2O4S.2H2O/c;;;;;4*1-5(2,3)4;;/h;4*1H3;4*(H2,1,2,3,4);2*1H2/q+4;;;;;;;;;;/p-4

InChI key

VCNAMBGKEDPVGQ-UHFFFAOYSA-J

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General description

Ammonium cerium(IV) sulfate dehydrate is a cerium salt widely used in the volumetric analysis.[1]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Self-Poled Transparent and Flexible UV Light-Emitting Cerium Complex-PVDF Composite: A High-Performance Nanogenerator.
Garain S, et al.
ACS Applied Materials & Interfaces, 7(2), 1298-1307 (2015)
David CA and Hellier DG
Dictionary of Environmentally Important Chemicals, 92-92 (1997)
Cerium-initiated grafting of acrylonitrile onto cellulosic materials.
Hebeish A and Mehta PC.
Journal of Applied Polymer Science, 12(7), 1625-1647 (1968)
Analysis of phenolic compounds in health care products by low-pressure liquid-chromatography with monolithic column and chemiluminescent detection.
Ballesta-Claver J, et al.
Luminescence, 26(1), 44-53 (2011)
K H Gordon et al.
Organic letters, 3(1), 53-56 (2001-06-30)
[figure: see text] A novel benzyloxyaniline linker that uses ceric ammonium nitrate (CAN) as a cleavage reagent is described. Its application in the solid-phase synthesis of N-unsubstituted beta-lactams and secondary amides furnishes compounds in moderate to excellent yield (45-91%) and

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